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Bifunctional aminosilane-functionalized Fe3O4 nanoparticles as efficient sorbent for preconcentration of cobalt ions from food and water samples

机译:双官能氨基硅烷官能化Fe3O4纳米粒子作为食物和水样中钴离子的前浓度的有效吸附剂

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摘要

Magnetic Fe3O4 nanoparticles were synthesized by a coprecipitation method, then their surface was covered and modified by [1-(2-aminoethyl)-3-aminopropyl]trimethoxysilane. The resulting adsorbent was used in preconcentration of Co(I (TM) I (TM)) ions prior to their determination by flame atomic absorption spectroscopy. The modified nanoparticles were characterized by Fourier-transform infrared spectroscopy, scanning electron microscopy, and vibrating-sample magnetometry techniques. Various parameters influencing the preconcentration efficiency, such as medium pH, adsorbent quantity, sample volume, and elution conditions, were optimized. Under optimum conditions, the analytical performance of the method was evaluated. The calibration curve was found to be linear from 1 to 200 mu g L-1 (R (2) = 0.99). The limit of detection was calculated to be 0.5 mu g L-1 (n = 5). The relative standard deviation was obtained as 2.5% (n = 5). Moreover, the maximum adsorption capacity of the sorbent was 32.05 mg g(-1). Kinetic and isotherm models were also studied, showing that the adsorption matched well with pseudo-second-order and Langmuir models. The ability of the developed method was proved by application for preconcentration of cobalt ions from food and water samples.
机译:通过共沉淀法合成磁Fe3O4纳米颗粒,然后通过[1-(2-氨基乙基)-3-氨基丙基]三甲氧基硅烷覆盖并改性它们的表面。得到的吸附剂在通过火焰原子吸收光谱法测定之前用于CO(I(TM)I(TM))离子的前浓缩。通过傅里叶变换红外光谱,扫描电子显微镜和振动样磁力技术的特征在于改性纳米颗粒。优化了影响前浓度的各种参数,例如培养基,吸附量,样品体积和洗脱条件。在最佳条件下,评估该方法的分析性能。发现校准曲线从1至200μgl-1的线性线性(R(2)= 0.99)。检测极限计算为0.5μgl-1(n = 5)。获得相对标准偏差为2.5%(n = 5)。此外,吸附剂的最大吸附容量为32.05mg(-1)。还研究了动力学和等温模型,表明吸附与伪二阶和Langmuir模型相匹配。通过施用来自食物和水样的钴离子的前浓度证明了开发方法的能力。

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